This technique, called enzyme-linked immunosorbent assay, is very sensitive, but it can take several days to carry out.

Elisa is short for "enzyme linked immunosorbent assay."

Enzyme-linked immunosorbent assay.

Examples include enzyme-linked immunosorbent assays.

This is done using the enzyme-linked immunosorbent assays (ELISA) method.

An enzyme linked immunosorbent assay (ELISA) test is available as well.

A slightly modified, sandwich enzyme-linked immunosorbent assay was used to examine the oxidative activities of caeruloplasmin in normal subjects and patients with Wilson's disease.

The enzyme-linked immunosorbent assay works by using antibodies immobilised on a microtiter plate to capture proteins of interest from samples added to the well.

Samples are tested through a technology known as enzyme linked immunosorbent assay (ELISA).

This may be with a laboratory test of the ELISA (enzyme-linked immunosorbent assay) type.

A new immunologic test, enzyme-linked immunosorbent assay (ELISA), is now available.

The Enzyme Linked Immunosorbent Assay has been used for decades to isolate and quantitatively measure proteins in samples.

A more advanced and reliable antibody method is known as Elisa, for Enzyme-Linked Immunosorbent Assay.

The most widely used and least expensive screening test for antibodies to HIV is the enzyme-linked immunosorbent assay (known as Elisa).

Enzyme-linked immunosorbent assay (ELISA) is a test that uses antibodies and color change to identify a substance.

Antigen-detection assays (e.g., enzyme-linked immunosorbent assay, immunochromatography) are available commercially that have good sensitivity and excellent specificity (485,486).

By raising Enzyme-linked immunosorbent assays against the nucleoproteins of symptomatic species, eight isolates have been identified in Italian vegetable and ornamental crops alone.

Enzyme linked immunosorbent assay is an assay that utilizes the principle of antibody-antigen recognition to test for the presence of certain substances.

Enzyme-linked immunosorbent assay (ELISA) uses antibodies to detect proteins and other different immunogens.

Of the 250,000-plus donors, there were 15 positives after repetitive Elisa (enzyme-linked immunosorbent assay) tests and confirmatory Western blot tests.

Optical density in all wells was measured by an enzyme-linked immunosorbent assay reader to minimise variability in interpretation and to eliminate errors in transcribing results.

Infectious retrovirus immunosorbent assay (IRISA)

Immunodiffusion, a modified direct complement-fixation test, and enzyme-linked immunosorbent assay also have been used successfully to detect antibody for PPV.

This value is known as the titer, and is most commonly determined through enzyme-linked immunosorbent assay (ELISA).

A common use for it is in the enzyme-linked immunosorbent assay (ELISA) to detect for binding of molecules to each other.